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Department of Biology
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An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability.
Human genetics Jul, 2016 | Pubmed ID: 27106595
Eif2b3 mutants recapitulate phenotypes of vanishing white matter disease and validate novel disease alleles in zebrafish.
Human molecular genetics Apr, 2021 | Pubmed ID: 33517449
Three-dimensional fluorescence microscopy through virtual refocusing using a recursive light propagation network.
Medical image analysis Nov, 2022 | Pubmed ID: 36116298
Chungnam National University
Eun-Seo Cho1,
Seungjae Han1,
Gyuri Kim1,
Minho Eom1,
Kang-Han Lee2,
Cheol-Hee Kim2,
Young-Gyu Yoon1,3
1School of Electrical Engineering, KAIST,
2Department of Biology, Chungnam National University,
3, KAIST Institute for Health Science and Technology
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